Exploration of an imide capture/N,N-acyl shift sequence for asparagine native peptide bond formation
Exploration of an imide capture/N,N-acyl shift sequence for asparagine native peptide bond formation
复制标题
天冬酰胺天然肽键形成的酰亚胺捕获/N,N-酰基移位序列的探索
DOI:
10.1016/j.bmc.2013.02.053
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发表时间:
2013
期刊:
影响因子:
--
通讯作者:
O.
中科院分区:
文献类型:
--
作者:
Mhidia;R.; Boll;E.; Fécourt;F.; Ermolenko;M.; Ollivier;N.; Sasaki;K.; Crich;D.; Delpech;B.; Melnyk;O.
Imide capture of a C-terminal peptidylazide with a side-chain thioacid derivative of an N-terminally protected aspartyl peptide leads to the formation of an imide bond bringing the two peptide ends into close proximity. Unmasking of the Nαprotecting group and intramolecular acyl migration results in the formation of a native peptide bond to asparagine.